Canonical Allele Identifier: CA107753976

Gene:

Linked Data

• dbSNP Id: rs547321139
• gnomAD v3: 4-144601485-C-T
• gnomAD v4: 4-144601485-C-T
• MyVariant Identifiers: chr4:g.145522637C>T (hg19) ; chr4:g.144601485C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144601485C>T , CM000666.2:g.144601485C>T	GRCh38
NC_000004.11:g.145522637C>T , CM000666.1:g.145522637C>T	GRCh37
NC_000004.10:g.145742087C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649263.1:c.328-185507G>A	ENSP00000497507.1:n.328-185507G>A